Craniodiaphyseal Dysplasia, Autosomal Dominant MeSH Supplementary Concept Data 2026

Details
Concepts

MeSH Supplementary: Craniodiaphyseal Dysplasia, Autosomal Dominant
Unique ID: C567275
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567275
Registry Numbers: 0
Heading Mapped to: *Osteochondrodysplasias; *Craniofacial Abnormalities
Frequency: 0
Date Introduced: 2012/11/05
Last Updated: 2012/11/05

Craniodiaphyseal Dysplasia, Autosomal Dominant Preferred

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